Abstract |
It has not been possible to determine the singular contribution of naive T lymphocytes to antigen-specific immunity after hematopoietic stem cell transplantation (HSCT), because of the confounding effects of donor-derived antigen-specific T lymphocytes present in most hematopoietic stem cell (HSC) products. Because umbilical cord blood contains only naive T lymphocytes, we longitudinally evaluated the recipients of unrelated cord blood transplantation (UCBT) for the presence of T lymphocytes with specificity for herpesviruses, to determine the contribution of the naive T lymphocytes to antigen-specific immune reconstitution after HSCT. Antigen-specific T lymphocytes were detected early after UCBT (herpes simplex virus on day 29; cytomegalovirus on day 44; varicella zoster virus on day 94). Overall, 66 of 153 UCBT recipients developed antigen-specific T lymphocytes to 1 or more herpesviruses during the evaluation period. The likelihood of developing antigen-specific T lymphocyte function was not associated with immunophenotypic T lymphocyte reconstitution, transplant cell dose, primary disease, or acute and chronic graft-versus-host disease. These results indicate that naive T lymphocytes present in the HSC inoculum can contribute to the generation of antigen-specific T-lymphocyte immunity early after transplantation.
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Authors | Geoff Cohen, Shelly L Carter, Kenneth I Weinberg, Bernadette Masinsin, Eva Guinan, Joanne Kurtzberg, John E Wagner, Nancy A Kernan, Robertson Parkman |
Journal | Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
(Biol Blood Marrow Transplant)
Vol. 12
Issue 12
Pg. 1335-42
(Dec 2006)
ISSN: 1083-8791 [Print] United States |
PMID | 17162216
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
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Topics |
- Adolescent
- Antibodies, Viral
(blood)
- Cell Lineage
- Child
- Child, Preschool
- Clinical Trials, Phase II as Topic
(statistics & numerical data)
- Cord Blood Stem Cell Transplantation
- Cytomegalovirus
(immunology, physiology)
- Cytomegalovirus Infections
(diagnosis, immunology, prevention & control, virology)
- False Negative Reactions
- Female
- Fetal Blood
(immunology)
- Follow-Up Studies
- Graft vs Host Disease
(etiology, immunology)
- Herpes Simplex
(diagnosis, immunology, prevention & control, virology)
- Herpes Zoster
(diagnosis, immunology, prevention & control, virology)
- Herpesvirus 3, Human
(immunology, physiology)
- Humans
- Infant
- Infant, Newborn
- Infections
(immunology, mortality)
- Male
- Multicenter Studies as Topic
(statistics & numerical data)
- Postoperative Complications
(immunology, mortality)
- Postoperative Period
- Simplexvirus
(immunology, physiology)
- T-Cell Antigen Receptor Specificity
- T-Lymphocyte Subsets
(immunology)
- Time Factors
- Treatment Outcome
- Virus Activation
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